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Centrifuge 5702

EUDAMED

Class A (EU MDR)

Ref 5702 000.329Ref 5702 000.019

by Eppendorf SE

Identity

Trade Name
Centrifuge 5702 EUDAMED
Device Name
Centrifuge 5702R; Centrifuge 5702RH; Centrifuge 5702 EUDAMED
Model / Reference
5702 000.329 EUDAMED
5702 000.019 EUDAMED

Identifiers

Primary DI / UDI-DI
04043758041334 EUDAMED
04043758029509 EUDAMED
Basic UDI-DI
04043758-IA-CEN-005-P4 EUDAMED
Direct Marketing DI
04043758041334 EUDAMED
04043758029509 EUDAMED
EMDN Code
W02069003 CENTRIFUGES EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

No

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

No

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

New Device

No

EUDAMED

Category: General-purpose centrifuge IVD

Centrifuge 5702 by Eppendorf SE — Class A — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose centrifuge IVD.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

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Manufacturer

Manufacturer
Eppendorf SE
EUDAMED SRN
DE-MF-000006237

Sources (2)

  • EUDAMED abdb6e81-ccd6-4a50-922f-73436b39813e 61 fields · synced Jul 11, 2026
  • EUDAMED e1bb7a5c-82ad-408f-b412-16c02af17db4 61 fields · synced May 18, 2026